Literature DB >> 3010860

Optimization of the BGM cell line culture and viral assay procedures for monitoring viruses in the environment.

D R Dahling, B A Wright.   

Abstract

An in-depth study of the continuous cell line designated BGM is described herein, and recommendations are made for standardizing cell culture and viral assay procedures. Based on data gathered from a survey of 58 laboratories using this cell line, a research plan was developed that included the study of growth media, sera, NaHCO3 levels, culture bottles, cell concentration, overlay media, agar, virus infection conditions, and cell-dissociating agents. Additionally, a comparative virus isolation study with BGM cells and nine other cell types was conducted with 37 sewage samples collected from nine different geographic areas. The results of the study indicated that the BGM cell line is superior for virus isolation when compared with the other cell types and that certain media and additives tend to increase BGM cell sensitivity to a specific group of viruses. A standardized procedure for cultivation of BGM cells is described which provides a more effective enterovirus assay system.

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Year:  1986        PMID: 3010860      PMCID: PMC238965          DOI: 10.1128/aem.51.4.790-812.1986

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  29 in total

1.  Propagation and isolation of group A coxsackieviruses in RD cells.

Authors:  N J Schmidt; H H Ho; E H Lennette
Journal:  J Clin Microbiol       Date:  1975-09       Impact factor: 5.948

2.  Survival of enteric viruses under natural conditions in a subarctic river.

Authors:  D R Dahling; R S Safferman
Journal:  Appl Environ Microbiol       Date:  1979-12       Impact factor: 4.792

3.  Use of a new bead microcarrier for the culture of anchorage dependent cells in pseudo suspension.

Authors:  D H Lewis; S A Volkers
Journal:  Dev Biol Stand       Date:  1979

4.  Buffer combinations for mammalian cell culture.

Authors:  H Eagle
Journal:  Science       Date:  1971-10-29       Impact factor: 47.728

5.  A survey of commercially available tissue culture media.

Authors:  H J Morton
Journal:  In Vitro       Date:  1970 Sep-Oct

6.  Routine enterovirus diagnosis in a human rhabdomyosarcoma cell line.

Authors:  E J Bell; B P Cosgrove
Journal:  Bull World Health Organ       Date:  1980       Impact factor: 9.408

7.  Viruses in sewage as an indicator of their presence in the community.

Authors:  J Sellwood; J V Dadswell; J S Slade
Journal:  J Hyg (Lond)       Date:  1981-04

8.  Relationship between in vitro growth promotion and biophysical and biochemical properties of the serum supplement.

Authors:  P J Price; E A Gregory
Journal:  In Vitro       Date:  1982-06

9.  Induction of cytopathogenicity in mammalian cell lines challenged with culturable enteric viruses and its enhancement by 5-iododeoxyuridine.

Authors:  W H Benton; R L Ward
Journal:  Appl Environ Microbiol       Date:  1982-04       Impact factor: 4.792

10.  Susceptibility of the VERO line of African green monkey kidney cells to human enteroviruses.

Authors:  P M Davis; R J Phillpotts
Journal:  J Hyg (Lond)       Date:  1974-02
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  22 in total

1.  Fortified sera and their use in environmental virology.

Authors:  J L Hoyt; A B Margolin
Journal:  Appl Environ Microbiol       Date:  2000-05       Impact factor: 4.792

2.  Presence of noroviruses and other enteric viruses in sewage and surface waters in The Netherlands.

Authors:  W J Lodder; A M de Roda Husman
Journal:  Appl Environ Microbiol       Date:  2005-03       Impact factor: 4.792

3.  Isolation and detection of enterovirus RNA from large-volume water samples by using the NucliSens miniMAG system and real-time nucleic acid sequence-based amplification.

Authors:  Saskia A Rutjes; Ronald Italiaander; Harold H J L van den Berg; Willemijn J Lodder; Ana Maria de Roda Husman
Journal:  Appl Environ Microbiol       Date:  2005-07       Impact factor: 4.792

4.  Detection of poliovirus by ICC/qPCR in concentrated water samples has greater sensitivity and is less costly using BGM cells in suspension as compared to monolayers.

Authors:  Helene B Balkin; Aaron B Margolin
Journal:  Virol J       Date:  2010-10-25       Impact factor: 4.099

5.  Long-term inactivation study of three enteroviruses in artificial surface and groundwaters, using PCR and cell culture.

Authors:  A M de Roda Husman; W J Lodder; S A Rutjes; J F Schijven; P F M Teunis
Journal:  Appl Environ Microbiol       Date:  2008-12-12       Impact factor: 4.792

6.  Use of propidium monoazide in reverse transcriptase PCR to distinguish between infectious and noninfectious enteric viruses in water samples.

Authors:  Sandhya Parshionikar; Ian Laseke; G Shay Fout
Journal:  Appl Environ Microbiol       Date:  2010-05-14       Impact factor: 4.792

7.  Efficacy of Nucleic Acid Probes for Detection of Poliovirus in Water Disinfected by Chlorine, Chlorine Dioxide, Ozone, and UV Radiation.

Authors:  N J Moore; A B Margolin
Journal:  Appl Environ Microbiol       Date:  1994-11       Impact factor: 4.792

8.  Presence of enteric viruses in source waters for drinking water production in The Netherlands.

Authors:  W J Lodder; H H J L van den Berg; S A Rutjes; A M de Roda Husman
Journal:  Appl Environ Microbiol       Date:  2010-07-09       Impact factor: 4.792

9.  Assessment of recovery efficiency of beef extract reagents for concentrating viruses from municipal wastewater sludge solids by the organic flocculation procedure.

Authors:  R S Safferman; M E Rohr; T Goyke
Journal:  Appl Environ Microbiol       Date:  1988-02       Impact factor: 4.792

10.  Concentration and purification of beef extract mock eluates from water samples for the detection of enteroviruses, hepatitis A virus, and Norwalk virus by reverse transcription-PCR.

Authors:  K J Schwab; R De Leon; M D Sobsey
Journal:  Appl Environ Microbiol       Date:  1995-02       Impact factor: 4.792

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